Living Transplant is a podcast that takes you behind the scenes at the transplant program at Toronto General Hospital with the goal to educate, inspire and fuel your passion about transplant, with your host, Candice Coghlan, an Education & Outreach Coordinator at the Centre for Living Organ Donation and kidney transplant recipient.
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PSC Mami: Stories at the intersection of PSC and parenthood. You are diagnosed with a rare, incurable disease. You are young. You had a vision for your future. You wanted kids. But can you? As a parent you want the best for your kids, but then they are diagnosed with PSC, what does their future hold? People who have been there talk about how a diagnosis of Primary Sclerosing Cholangitis, a rare autoimmune disease, reshaped their vision of their lives and parenthood.
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In this episode of the Living Transplant podcast, host Candice Coghlan is joined by Winne Jerome who talks to us about her journey as a living donor to her sister through the Kidney Paired Donation Program, making that decision after having a premature newborn baby at home. She spoke about how when she found out she was able to donate a kidney to a…
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In this episode of the Living Transplant postcast, host, Candice Coghlan was joined by Stephanie Dyriw, a living liver donor to her son. Stephanie was put in a situation no parent could ever imagine, when her healthy, three and a half year old son crashed into liver failure with no warning. Within days, Stephanie and the UHN team worked tirelessly …
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In this episode of the Living Transplant podcast, host, Candice Coghlan, was joined by Manuel Escoto, the Patient, Family, Donor Partnerships and Knowledge Mobilization Director at CDTRP, the Canadian Donation and Transplantation Research Program alongside Sadia Baig, the Programs Coordinator at the Kidney Foundation of Canada, Ontario branch. What…
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It's Not Outrageous: Jillian Best's Epic Swim Across Lake Ontario
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In this episode of the Living Transplant podcast, host Candice Coghlan was joined by Jillian Best, the first organ transplant recipient and one in only 72 people to ever swim across Lake Ontario in all of recorded history. Jillian trained, swam and built her mental fortitude so she could swim across Lake Ontario in 18 hours and 36 minutes. She fini…
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I Don’t Want to Just Survive, I Want to Live
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In this episode of the Living Transplant podcast, host Candice, was joined by Dawn Ethier, a police officer and mother of four. Dawn had thyroid cancer over 10 years ago. The cancer was treated, but she was left with hypoparathyroidism, which caused horrible side effects, changed her lifestyle, and took a lot of time away from her family, her work,…
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In this episode of the Living Transplant podcast, host Candice Coghlan was joined by Kelsey Hannah, an OR nurse and mother who went on a journey of health and wellness to lose weight to save her mother's life by donating a portion of her liver to her. We talked about her journey of self reflection, empowerment, dedication, and what it felt like to …
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WELCOME TO SEASON 5! In this episode, host Candice Coghlan was joined by Vanessa Tait, a Cree woman from O-Pipon-Na-Piwin Cree Nation who put her heart and soul into supporting her father, Kenneth, through his kidney health journey. She uprooted their lives to move from her father's home community of O-Pipon-Na-Piwin Cree Nation, over 700km north o…
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In this episode, host, Candice, is joined by Melissa Sidhu who works in healthcare, is a passionate volunteer and living liver donor to her brother over 10 years ago. We spoke about her journey as a donor, relationships with loved ones, how to find tiny moments of joy and gratitude throughout this episode. You will also hear clips from members of t…
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In this episode, host Candice Coghlan sat down with Afsana Lallani, a cat lover and nursing graduate who made a public social appeal to find a living liver donor to save her life. They talk about being young and living with a chronic illness, facing death and how a supportive community can make all the difference. They are later joined by Dilshad L…
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In this episode, we're celebrating Living Donation Week. Host, Candice was joined by Sylvie Charbonneau, past president of the Kidney Foundation of Canada, advocate, change maker, and living kidney donor to her son. We were also joined by Dr. Joseph Kim, Director of the Kidney Transplant Program at the Ajmera Transplant Center. We discussed barrier…
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Ajmera Transplant Centre's 2nd Annual Education & Research Conference
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In this episode, host Candice, takes you behind the scenes of the Ajmera Transplant Centre's 2nd Annual Education and Research Conference, to hear about incredible science, clinical, and research aspects of transplantation. Hear from the following: Samrat Ray: Expanding the transplant pancreas donor, using an ex vivo perfusion model. Adriana Robert…
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I've done this before, I can do it again.
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In this episode, host Candice Coghlan was joined by Justin Poy, a father, entrepreneur, and businessman who has lived with multiple types of renal replacement therapy since the age of 10, including three kidney transplants, hemodialysis, peritoneal dialysis, as well as home dialysis. Justin spoke about mental health, resiliency, parenting with a ch…
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In this episode, host Candice Coghlan sat down with Tara Lisabeth, who received not one, but two double lung transplants at a young age. She spoke about life with cystic fibrosis, what it felt like to take deep breaths and how transplant gave her the opportunity to walk down the aisle and get married. Later we were joined by Dr. Marcelo Cypel, the …
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In this episode host, Candice Coghlan sat down with Craig Lindsay, the Senior Manager of Programs and Public Policy for the Kidney Foundation of Canada, Ontario Branch. Craig not only works tirelessly supporting this community, but he's also part of it, having lived with diabetes, which eventually caused his kidneys to fail. Craig did home dialysis…
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In this episode, host Candice Coghlan sat down with Shilpa Raju, an epidemiologist who finished her degree while battling cancer. She survived the cancer, however unfortunately the side effects from her treatment caused severe lung damage, resulting in her need for a double lung transplant. Shilpa spoke about being a young person battling illness a…
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Host Candice Coghlan is joined by Darryl Wallis, who was diagnosed with Hollow Visceral Myopathy at age one. He grew up in and out of hospitals and unable to eat, but about 16 years ago, he received a multi-organ transplant including a liver, bowel, stomach and pancreas, which gave him his life back. He was able to have a family and become a pharma…
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Host Candice Coghlan is joined by Amber Needham and her living eye stem cell donor, Kathy O'Toole. They discuss how Amber lost her eyesight twice from unique situations. Amber, Kathy and Candice talk about their remarkable journey as Amber went from 2020 vision to blindness and how she was given a second chance with sight when Kathy donated stem ce…
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Host Candice Coghlan is joined by Ivica, an opera singer who loves baking, teaching others, and above all else, his family. Ivica discusses his journey with kidney failure and how his brother stepped forward to be his donor, giving him back the strength to sing beautifully. Later we're joined by Margot Mitchell, a retired social worker who worked a…
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Host Candice Coghlan is joined by Charles Cook, an incredibly brave and vibrant person who is a heart and kidney transplant recipient. After far too many close cases with death, Charles has implemented the life motto of ‘keep bangin’. Charles and Candice are later joined by the one of a kind cardiologist, Dr. Heather Ross who is highly decorated wi…
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In September, 2022, we launched Great Actions Leave a Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients from across Canada. This week you will hear another story from a great actions model about their journey with living o…
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In September 2022, we launched Great Actions Leave a Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients across Canada. In this episode, Host Candice is joined by Ian Goodall-George, who self proclaimed himself as the poster…
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BONUS: Great Actions Leave a Mark - Ashley
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In September 2022, we launched Great Actions Leave a Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients across Canada. In this episode, Host Candice is joined by Ashley, a world traveller and horseback rider who donated a k…
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BONUS: Great Actions Leave a Mark - Craig
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In September, 2022, we launched Great Actions Leave A Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients across Canada. In the coming weeks, you'll hear stories from great actions models about their journey with living orga…
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BONUS: Great Actions Leave a Mark - Jaime
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Bonus Episode: Great Actions Leave a Mark - Jaime In September, 2022, we launched Great Actions Leave A Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients across Canada. In the coming weeks, you'll hear stories from Great A…
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BONUS EPISODE: Remember This Living Donation - Len
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Bonus Episode: Remember This Living Donation - Len During Living Donation Week 2021, we partnered with the podcast, Remember This, with host Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Len shares his story as a double anonymous, non-directed living donor, which means he don…
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BONUS EPISODE: Remember This Living Donation - Glenna
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Bonus Episode: Remember This- Glenna During Living Donation Week 2021, we partnered with the podcast, Remember This, with host Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Glenna shares her journey as a non-directed, living anonymous donor, meaning she donated 62% of her liv…
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BONUS EPISODE: Remember This Living Donation - Katie
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During Living Donation Week 2021, we partnered with the podcast, Remember This, hosted by Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Katie shares her journey as a living liver donor to her husband Simon and its impact on their family. Enjoy! To submit your story, please re…
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BONUS EPISODE: Remember This Living Donation - Palma
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Bonus Episode: Remember This- Palma During Living Donation Week 2021, we partnered with the podcast, Remember This, with host Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Palma shares her journey as a living liver donor to her cousin Jess. Enjoy! The views and opinions expre…
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Host Candice Coghlan is joined by Natalie Theron, a liver transplant recipient who was diagnosed with stage four colon cancer the day before she gave birth to her daughter. After an incredible journey with cancer trials, chemotherapy, a HAIP pump and hospital stays, Natalie’s husband became her liver donor, effectively curing her liver cancer. Cand…
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Host Candice Coghlan is joined by Team Delfina: Betsy Amores, Peter Budziak and their two amazing children, liver transplant recipient Delfina, and big brother Matthew. Peter and Betsy talk about their family’s journey with Delfina, who was diagnosed with biliary atresia, and later needed a living liver transplant to save her life. After a large me…
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Ordinary People Can Do Extraordinary Things
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Host Candice Coghlan is joined by guest host, Ioanna Roumeliotis, a kidney donor to her brother who lives with Polycystic Kidney Disease. They discuss the process of donating, the ups and downs and how ordinary people can do extraordinary things, like saving a life by donating a kidney or liver. Candice and Ioanna are joined by Dr. Sunita Singh, Me…
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Host Candice Coghlan is joined by guest host, Maria Acero. They discuss Maria’s journey as a caregiver to her husband Luis, who was diagnosed with autoimmune hepatitis at the age of 15, and at the age of 47, was diagnosed with hepatocellular carcinoma. In 2019, Luis underwent two liver transplants within nine days, saving his life, but leaving him …
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Behind the Scenes at the Banff CST Conference
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This is a special episode of Behind the Scenes at the Banff CST Conference. The conference connects members of the Canadian Society of Transplantation with cutting edge science and leading clinical practices that can be used to advance the practice and science of transplantation in Canada. Host Candice Coghlan is joined by members who presented at …
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There isn’t a heart sitting on a shelf waiting.
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Host Candice Coghlan is joined by guest host, Michelle Rambarran. They discuss Michelle’s journey as a new mom, learning she had spontaneous coronary artery dissection and what it was like to have a heart transplant, fearing that she may not see her son’s first birthday. Michelle had twelve amazing years with her heart, but needed a second heart tr…
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Host Candice Coghlan is joined by guest host, Chris Smith. Chris discusses how he became involved as an organ donation advocate through meeting his partner after she donated a portion of her liver to her father. Candice and Chris are joined by Dr. Markus Selzner, the Surgical Director of the Ajmera Liver Transplant Program at the University of Toro…
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Two Bellybuttons and the End of the Wait List
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Host Candice Coghlan is joined by guest hosts Joanne Kearney and Brendan Cahill, co-founders of the Centre for Living Organ Donation to tell their story of how Brendan became a kidney donor to Joanne through the Paired Exchange Program and how they used math to support their decisions and later pivoted to channel their passion and experience to hel…
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Host Candice Coghlan is joined by guest host, Mary Beaucage. As a follow up to the episode Indigenous Ways of Knowing, Mary discusses her kidney transplant from her cousin, barriers to transplant and her extensive advocacy work. Candice and Mary are joined by Dr. Istvan Mucsi, a clinical investigator and transplant nephrologist at the Multi Organ T…
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If you’re going through hell, keep going
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Host Candice Coghlan is joined by guest host, Alley Adams who lived with type 1 diabetes for over 30 years, and after three calls, received a kidney pancreas transplant on her fourth. They speak about what it is like to be diagnosed with a chronic illness at a young age, how that impacts your outlook on life, and how to find a living donor. Alley a…
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Host Candice Coghlan is joined by Guest Host, Sara Murray, who was diagnosed with cystic fibrosis at just months old. She brings us through her brave journey of what life was like as a child and young adult with cystic fibrosis and what it was like to receive “the call” for her lung transplant. Sara also discusses her journey in wanting to become a…
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Today’s episode contains material that might be difficult to hear. Discretion is advised. Host Candice Coghlan is joined by guest host, Tamara Hartley- Harris who was diagnosed with type 1 diabetes at a young age. Tamara’s journey is one that is filled with hardship, strength and love. She discusses living with diabetes, having a life-threatening h…
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Host Candice Coghlan is joined by guest host, Kate Chong, who received a kidney transplant from her husband. Kate and her husband have a two year old daughter, and she is pregnant, excitedly awaiting the birth of her son. Candice and Kate discuss their journeys in family planning, being pregnant, and the joys of motherhood while living with chronic…
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Joanne found community and mission after her son was diagnosed with pediatric PSC over 15 years ago Joanne’s son was diagnosed with Primary Sclerosing Cholangitis at 15 and she has walked the journey with him for over a decade and a half. In doing so, she not only advocates for him but for all PSCers in her work with PSC Partners Seeking a Cure. Sh…
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Stuart makes life changes after PSC diagnosis to spend more time with his family Stuart made a conscious decision to make time for his children and spouse when his Primary Sclerosing Cholangitis diagnosis focused him on what was important in his life. He shares about what it’s like to be the financial provider for his family, the essential role his…
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Laura realigned her life after her diagnosis of Primary Sclerosing Cholangitis. She refocused on family, friends, fun and her dream of becoming an author. Her writing served many purposes at different times, including as long letters to her three daughters, to escape from illness and as a tool for healing. Post-liver transplant, she and her family …
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Jennifer’s experience with organ transplantation comes full circle from agreeing to donate a loved ones organs to being the recipient of part of her husband’s liver through a living donor transplant. She shares her struggles with end-stage autoimmuneBy Monika Aldarondo
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Nicola finds meaning in advocacy after her transplant, post-transplant pregnancy, and surrogacy journey. Family is central to Nicola’s journey. Her younger brother was her donor for her life saving transplant in her 20s. She now focuses on raising her two young sons and creating joyful memories with them. She also works to instill empathy and gener…
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Indigenous Ways of Knowing: Kidney Transplant
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Hosts Courtney and Brittany sit down with Indigenous storyteller and kidney transplant recipient, Mary Beaucage for an authentic look at the kidney transplant experience. From her crash start into kidney failure to new experiences of community to advocating for patient oriented research, Mary holds nothing back. Read more about Mary’s transplant pa…
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Courtney and Brittany sit down with Tianna McFarlane, the founder of Heal in Colour, for something a little different but absolutely necessary. Launched earlier this year, Heal in Colour is revolutionizing the way people shop for bandages by creating a world where black and brown bandages are part of the norm. Find out how Tianna broke into bandage…
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Post-liver transplant coordinator, Shauna Watson and post-lung transplant coordinator, Pauline Harney join Courtney and Brittany to discuss their roads into the world of transplant, the day-to-day life of a coordinator, and how they stay organized with literally hundreds of patients. Shauna and Pauline talk about the joy of seeing patients thrive a…
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Courtney and Brittany are joined by Dr. Hance Clarke, Director of Pain Services and Medical Director of the Pain Research Unit at Toronto General Hospital. Dr. Clarke walks our hosts through his journey to pain medicine, the difference between acute pain services and transitional pain services, and the interaction between CBD, THC, and anti-rejecti…
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